Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Femoral Segment,in combination with Size 4
WALDEMAR LINK GmbH & Co. KG
15-2976/20
In Commercial Distribution

  • 04026575328352 ()
15-2976/20

  • Knee arthroplasty wedge
Femoral Segment,in combination with Size 4
WALDEMAR LINK GmbH & Co. KG
15-2976/10
In Commercial Distribution

  • 04026575328345 ()
15-2976/10

  • Knee arthroplasty wedge
Femoral Segment,in combination with Size 4
WALDEMAR LINK GmbH & Co. KG
15-2970/10
In Commercial Distribution

  • 04026575205929 ()
15-2970/10

  • Knee arthroplasty wedge
Femoral Segment,in combination with Size 4
WALDEMAR LINK GmbH & Co. KG
15-2970/20
In Commercial Distribution

  • 04026575205936 ()
15-2970/20

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT MD/MD+ NON-POROUS
Microport Orthopedics Inc.
18723004
In Commercial Distribution

  • 18723004 ()
  • M684187230041 ()
18723004

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 7 SMALL
Smith & Nephew, Inc.
71520071
Not in Commercial Distribution

  • 03596010228147 ()
71520071

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 6 SMALL
Smith & Nephew, Inc.
71520061
Not in Commercial Distribution

  • 03596010228109 ()
71520061

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 5 SMALL
Smith & Nephew, Inc.
71520051
Not in Commercial Distribution

  • 03596010228062 ()
71520051

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 4 SMALL
Smith & Nephew, Inc.
71520041
Not in Commercial Distribution

  • 03596010228024 ()
71520041

  • Knee arthroplasty wedge
PROFIX NON-POROUS FEMORAL WEDGE SIZE 3 LARGE
Smith & Nephew, Inc.
71520032
Not in Commercial Distribution

  • 03596010227997 ()
71520032

  • Knee arthroplasty wedge
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